TRABAJO STUDY START UP

Senior study start up associate - multilingual icon plc is a world-leading healthcare intelligence and clinical research organization... minimum of 2 years of experience...

May be involved in activities related to monthly study budget planning and reviews... execute operational strategy/ expectations for maintenance of clinical study...

Puedes asumir múltiples tareas al mismo tiempo manteniendo la calma... creamos piezas que permiten a nuestros clientes explorar creativamente su individualidad...

Establish and maintain methods to initiate study start up planning... track study start up progress and provide regular updates to gco ccs management team and cross...

Day to day responsibilities will include: support clinical research studies and maintain a safe study environment according to health and safety policies under...

Day to day responsibilities will include: support clinical research studies and maintain a safe study environment according to health and safety policies under the...

Certified veeva study builders preferred... minimum 2 years of experience in veeva cdms study build... ability to manage multiple study builds and post-release changes...

Management of study documentation communication with sponsors and cros... at least six months of experience as study coordinator or data entry...

Willingness to travel up to 10% of the time... role overview: we are seeking a clinical study coordinator to join our team... we are looking for a clinical study...

After reviewing the content of the applications, the panel will start the interviews, with at least one technical and one administrative interview...

We want to set you up for success in your job, and an important part of that includes comprehensive perks & benefits... support new business territory sizing...

Interpretation of study data and scientific content of clinical study reports (csrs) and regulatory submissions...   presents the scientific rationale and study...

Key responsibilities: study start-up and study conduct activities including drafting icf study specific template and tmf plan, approving study specific essential...

Expertise in study conduct, follow up and monitoring advanced knowledge of clinical and outcomes research study design... identify site successes and challenges...

    start date: april 1st leads/contributes to the preparation of delegated study documents (e... informed consent form, master clinical study agreement...

Implementation of study amendment-and changes in study related processes)... as required, manages the local study supply... drive study compliance by maintaining...